针对软疣病毒加工因子的小分子与三肽共轭后效力增强

IF 4.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Hancheng Guan , Manunya Nuth , Richard W. Scott , Michael H. Parker , Eric D. Strobel , Allen B. Reitz , John L. Kulp III , Robert P. Ricciardi
{"title":"针对软疣病毒加工因子的小分子与三肽共轭后效力增强","authors":"Hancheng Guan ,&nbsp;Manunya Nuth ,&nbsp;Richard W. Scott ,&nbsp;Michael H. Parker ,&nbsp;Eric D. Strobel ,&nbsp;Allen B. Reitz ,&nbsp;John L. Kulp III ,&nbsp;Robert P. Ricciardi","doi":"10.1016/j.antiviral.2024.105899","DOIUrl":null,"url":null,"abstract":"<div><p>We recently developed compound <strong>FC-7269</strong> for targeting the Molluscum contagiosum virus processivity factor (mD4) and demonstrated its ability to inhibit viral processive DNA synthesis <em>in vitro</em> and cellular infection of an mD4-dependent virus (<em>Antiviral Res 211, 2023,105520</em>). However, despite a thorough medicinal chemistry campaign we were unable to generate a potent second analog as a requisite for drug development. We overcame this impasse, by conjugating a short hydrophobic trivaline peptide to <strong>FC-7269</strong> to produce <strong>FC-TriVal-7269</strong> which significantly increased antiviral potency and reduced cellular toxicity.</p></div>","PeriodicalId":8259,"journal":{"name":"Antiviral research","volume":null,"pages":null},"PeriodicalIF":4.5000,"publicationDate":"2024-05-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Potency of a small molecule that targets the molluscum contagiosum virus processivity factor increases when conjugated to a tripeptide\",\"authors\":\"Hancheng Guan ,&nbsp;Manunya Nuth ,&nbsp;Richard W. Scott ,&nbsp;Michael H. Parker ,&nbsp;Eric D. Strobel ,&nbsp;Allen B. Reitz ,&nbsp;John L. Kulp III ,&nbsp;Robert P. Ricciardi\",\"doi\":\"10.1016/j.antiviral.2024.105899\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We recently developed compound <strong>FC-7269</strong> for targeting the Molluscum contagiosum virus processivity factor (mD4) and demonstrated its ability to inhibit viral processive DNA synthesis <em>in vitro</em> and cellular infection of an mD4-dependent virus (<em>Antiviral Res 211, 2023,105520</em>). However, despite a thorough medicinal chemistry campaign we were unable to generate a potent second analog as a requisite for drug development. We overcame this impasse, by conjugating a short hydrophobic trivaline peptide to <strong>FC-7269</strong> to produce <strong>FC-TriVal-7269</strong> which significantly increased antiviral potency and reduced cellular toxicity.</p></div>\",\"PeriodicalId\":8259,\"journal\":{\"name\":\"Antiviral research\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2024-05-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Antiviral research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0166354224001086\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Antiviral research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0166354224001086","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

摘要

我们最近开发了针对传染性软疣病毒过程因子(mD4)的化合物 FC-7269,并证明了其在体外抑制病毒过程 DNA 合成和抑制依赖 mD4 病毒的细胞感染的能力(Antiviral Res 211, 2023,105520)。然而,尽管我们进行了全面的药物化学研究,但仍无法生成药物开发所需的强效第二类似物。我们克服了这一僵局,在 FC-7269 上连接了一个短的疏水三价肽,生成了 FC-TriVal-7269,显著提高了抗病毒效力并降低了细胞毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Potency of a small molecule that targets the molluscum contagiosum virus processivity factor increases when conjugated to a tripeptide

We recently developed compound FC-7269 for targeting the Molluscum contagiosum virus processivity factor (mD4) and demonstrated its ability to inhibit viral processive DNA synthesis in vitro and cellular infection of an mD4-dependent virus (Antiviral Res 211, 2023,105520). However, despite a thorough medicinal chemistry campaign we were unable to generate a potent second analog as a requisite for drug development. We overcame this impasse, by conjugating a short hydrophobic trivaline peptide to FC-7269 to produce FC-TriVal-7269 which significantly increased antiviral potency and reduced cellular toxicity.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Antiviral research
Antiviral research 医学-病毒学
CiteScore
17.10
自引率
3.90%
发文量
157
审稿时长
34 days
期刊介绍: Antiviral Research is a journal that focuses on various aspects of controlling viral infections in both humans and animals. It is a platform for publishing research reports, short communications, review articles, and commentaries. The journal covers a wide range of topics including antiviral drugs, antibodies, and host-response modifiers. These topics encompass their synthesis, in vitro and in vivo testing, as well as mechanisms of action. Additionally, the journal also publishes studies on the development of new or improved vaccines against viral infections in humans. It delves into assessing the safety of drugs and vaccines, tracking the evolution of drug or vaccine-resistant viruses, and developing effective countermeasures. Another area of interest includes the identification and validation of new drug targets. The journal further explores laboratory animal models of viral diseases, investigates the pathogenesis of viral diseases, and examines the mechanisms by which viruses avoid host immune responses.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信